Journal article

Enantiomerically enriched trans-diols from alkenes in one pot: a multicatalyst approach


Authors listHrdina, R; Müller, CE; Wende, RC; Wanka, L; Schreiner, PR

Publication year2012

Pages2498-2500

JournalChemical Communications

Volume number48

Issue number19

DOI Linkhttps://doi.org/10.1039/C2CC17435A

PublisherRoyal Society of Chemistry


Abstract

Multicatalysts consisting of non-natural oligopeptides with distinctly different catalytic moieties create molecular complexity in a multistep one-pot sequence starting from simple alkenes yielding highly enantiomerically enriched trans-diols.




Citation Styles

Harvard Citation styleHrdina, R., Müller, C., Wende, R., Wanka, L. and Schreiner, P. (2012) Enantiomerically enriched trans-diols from alkenes in one pot: a multicatalyst approach, Chemical Communications, 48(19), pp. 2498-2500. https://doi.org/10.1039/C2CC17435A

APA Citation styleHrdina, R., Müller, C., Wende, R., Wanka, L., & Schreiner, P. (2012). Enantiomerically enriched trans-diols from alkenes in one pot: a multicatalyst approach. Chemical Communications. 48(19), 2498-2500. https://doi.org/10.1039/C2CC17435A


Last updated on 2025-21-05 at 15:22